DISEASES

Disease-gene associations mined from literature

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Human genes for multiple endocrine neoplasia type 2A

Multiple endocrine neoplasia type 2A [DOID:0050430]

An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis.

Synonyms:  multiple endocrine neoplasia type 2A,  DOID:0050430,  MEN2A,  Sipple syndrome,  multiple endocrine neoplasia II ...

Linkouts:  OMIM

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Albert Pallejà, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.